Benzaldehyde → 3-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dione

HRID 517612

반응식

HRID 517612 반응식
C(=O)C1C=CC=CC=1.C(NCCN1C(=O)CSC1=O)(C1C=CC=CC=1)(C1C=CC=CC=1)C1C=CC=CC=1.N1CCCCC1.[NH2:44][CH2:45][CH2:46][N:47]1[C:51](=[O:52])[CH:50]([CH2:53][C:54]2[CH:59]=[CH:58][C:57](OCC)=[CH:56][CH:55]=2)[S:49][C:48]1=[O:63]>C(O)C>[NH2:44][CH2:45][CH2:46][N:47]1[C:51](=[O:52])/[C:50](=[CH:53]/[C:54]2[CH:59]=[CH:58][CH:57]=[CH:56][CH:55]=2)/[S:49][C:48]1=[O:63]

참가 물질

6

반응물 4

HCID 240BenzaldehydeHCID 8082PiperidineHCID 716970713-(2-Aminoethyl)-5-(4-ethoxybenzyl)thiazolidine-2,4-dioneHCID 716971683-(2-(Tritylamino)ethyl)thiazolidine-2,4-dione

생성물 1

HCID 15512443-(2-Aminoethyl)-5-(phenylmethylidene)-1,3-thiazolidine-2,4-dione수율 48.1%

시약·촉매·용매 1

HCID 702Ethanol용매

반응 조건

온도
75 °C

실험 절차

Benzaldehyde (63 μL, 0.62 mmol) and compound 29 (250 mg, 0.62 mmol) were dissolved in 10 mL of anhydrous ethanol at room temperature, and piperidine (7 μL, 0.062 mmol) was added to the reaction solution. The reaction mixture was stirred at 75° C. for 1 day and then allowed to cool down to room temperature until a yellow crystalline precipitate formed, and the solid was collected by filtration, washed with water and ethyl acetate, and dried to afford a white solid. Deprotection following the procedure of compound 6 gave the title compound 30a as a white solid (48.1%, 74 mg).

후처리

  1. temperatureto cool down to room temperature until a yellow crystalline precipitate
  2. customformed
  3. filtrationthe solid was collected by filtration
  4. washwashed with water and ethyl acetate
  5. customdried
  6. customto afford a white solid

출처 및 근거

ORD 기록
ord-1c0a01a673f2498fba074e97cbe46588
출처 데이터셋
uspto-grants-2015_08
특허 번호
US09115122B2

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